Do you have 10 minutes to help shape the future of OA/TOF support?
EAT – the federation of Esophageal Atresia Global Support Groups (of which TOFS is a founding member) is conducting a global survey to better understand the needs of those born with OA/TOF.
Please take this opportunity to ensure that international medical experts hear the patient perspective loud and clear.
What you need to know:
- Who should complete the survey: those born with OA/TOF or the parents/caregivers of children born with OA/TOF.
- Time to complete: under 10 minutes.
- Goal: to gain a clearer understanding of the experiences, challenges, and needs of individuals and families living with oesophageal atresia worldwide.
Your contribution will help EAT advocate more effectively, improve support, and ensure that the patient and family perspective is heard by international experts.
Participation is voluntary but makes a world of difference.
If you have any questions or would like to have more information, please feel free to contact EAT at survey@eat-federation.org or visit www.eat-federation.org
Thank you for your support.
